Related references
Note: Only part of the references are listed.STEM CELLS AND THE DIFFERENTIATION HIERARCHY IN MAMMARY GLAND DEVELOPMENT
Nai Yang Fu et al.
PHYSIOLOGICAL REVIEWS (2020)
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Daniel R. Barnes et al.
GENETICS IN MEDICINE (2020)
Genomic Signatures Predict the Immunogenicity of BRCA-Deficient Breast Cancer
Adam A. Kraya et al.
CLINICAL CANCER RESEARCH (2019)
Mammary stem cells and progenitors: targeting the roots of breast cancer for prevention
Pirashaanthy Tharmapalan et al.
EMBO JOURNAL (2019)
Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients
Andre Kahles et al.
CANCER CELL (2018)
Accurate classification of BRCA1 variants with saturation genome editing
Gregory M. Findlay et al.
NATURE (2018)
GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers
Fabienne Lesueur et al.
FRONTIERS IN ONCOLOGY (2018)
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Karoline B. Kuchenbaecker et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2017)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou et al.
NATURE (2017)
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Roger L. Milne et al.
NATURE GENETICS (2017)
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Karoline B. Kuchenbaecker et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2017)
Nanopore sequencing of full-length BRCA1 mRNA transcripts reveals co-occurrence of known exon skipping events
Lucy C. de Jong et al.
BREAST CANCER RESEARCH (2017)
Modifiers of breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers
Roger L. Milne et al.
ENDOCRINE-RELATED CANCER (2016)
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms
Miguel de la Hoya et al.
HUMAN MOLECULAR GENETICS (2016)
An Integrated Genome-Wide Systems Genetics Screen for Breast Cancer Metastasis Susceptibility Genes
Ling Bai et al.
PLOS GENETICS (2016)
BRCA1 Alternative splicing landscape in breast tissue samples
Atocha Romero et al.
BMC CANCER (2015)
SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition
Eunhee Kim et al.
CANCER CELL (2015)
Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
Timothy R. Rebbeck et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2015)
Comprehensive annotation of splice junctions supports pervasive alternative splicing at the BRCA1 locus: a report from the ENIGMA consortium
Mara Colombo et al.
HUMAN MOLECULAR GENETICS (2014)
BRCA1 Exon 11, a CERES (Composite Regulatory Element of Splicing) Element Involved in Splice Regulation
Claudia Tammaro et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2014)
BRCA1 exon 11 a model of long exon splicing regulation
Michela Raponi et al.
RNA BIOLOGY (2014)
Risk determination and prevention of breast cancer
Anthony Howell et al.
BREAST CANCER RESEARCH (2014)
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen et al.
NATURE (2013)
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Fergus J. Couch et al.
PLOS GENETICS (2013)
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
Mia M. Gaudet et al.
PLOS GENETICS (2013)
Parity induces differentiation and reduces Wnt/Notch signaling ratio and proliferation potential of basal stem/progenitor cells isolated from mouse mammary epithelium
Fabienne Meier-Abt et al.
BREAST CANCER RESEARCH (2013)
BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer
Claudia Tammaro et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2012)
SpliceAid 2: A Database of Human Splicing Factors Expression Data and RNA Target Motifs
Francesco Piva et al.
HUMAN MUTATION (2012)
An integrated encyclopedia of DNA elements in the human genome
Ian Dunham et al.
NATURE (2012)
Evolutionary Constraint Helps Unmask a Splicing Regulatory Region in BRCA1 Exon 11
Michela Raponi et al.
PLOS ONE (2012)
Evolutionary Pathways in BRCA1-Associated Breast Tumors
Filipe C. Martins et al.
CANCER DISCOVERY (2012)
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
David G. Cox et al.
HUMAN MOLECULAR GENETICS (2011)
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Antonis C. Antoniou et al.
NATURE GENETICS (2010)
BRCA1 and its toolbox for the maintenance of genome integrity
Michael S. Y. Huen et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2010)
Regulation of Alternative Splicing by Histone Modifications
Reini F. Luco et al.
SCIENCE (2010)
Unclassified variants identified in BRCA1 exon 11:: Consequences on splicing
Olga Anczukow et al.
GENES CHROMOSOMES & CANCER (2008)
A Large Fraction of Unclassified Variants of the Mismatch Repair Genes MLH1 and MSH2 Is Associated With Splicing Defects
Isabelle Tournier et al.
HUMAN MUTATION (2008)
RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers:: Results from a combined analysis of 19 studies
Antonis C. Antoniou et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Key stages in mammary gland development - Secretory activation in the mammary gland: it's not just about milk protein synthesis!
Steven M. Anderson et al.
BREAST CANCER RESEARCH (2007)
RNA-based analysis of BRCA1 and BRCA2 gene alterations
Fabrizia Bonatti et al.
CANCER GENETICS AND CYTOGENETICS (2006)
Hyperplasia and spontaneous tumor development in the gynecologic system in mice lacking the BRCA1-Δ11 isoform
Sang Soo Kim et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Dynamics of DNA repair suggested by the subcellular localization of Brca1 and Brca2 proteins
LJ Huber et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2005)
A haplotype-based case-control study of BRCA1 and sporadic breast cancer risk
ML Freedman et al.
CANCER RESEARCH (2005)
Haploview: analysis and visualization of LD and haplotype maps
JC Barrett et al.
BIOINFORMATICS (2005)
Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer
DG Cox et al.
BREAST CANCER RESEARCH (2005)
A requirement for breast-cancer-associated gene 1 (BRCA1) in the spindle checkpoint
RH Wang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer
WD Foulkes et al.
JOURNAL OF THE NATIONAL CANCER INSTITUTE (2003)
ESEfinder: a web resource to identify exonic splicing enhancers
L Cartegni et al.
NUCLEIC ACIDS RESEARCH (2003)
Senescence aging, and malignant transformation mediated by p53 in mice lacking the Brcal full-length isoform
L Cao et al.
GENES & DEVELOPMENT (2003)
Retroviral transduction of splice variant Brca1-Delta 11 or mutant Brca1-W1777Stop causes mouse epithelial mammary atypical duct hyperplasia
R Bachelior et al.
VIRCHOWS ARCHIV (2002)
Genetic interactions between tumor suppressors Brca1 and p53 in apoptosis, cell cycle and tumorigenesis
XL Xu et al.
NATURE GENETICS (2001)
Expression profiles of BRCA1 splice variants in asynchronous and in G1/S synchronized tumor cell lines
TI Orban et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)